Polystyrene Core Research Articles

Rh nanoparticles confined in triphenylphosphine oxide-functionalized core-crosslinked micelles with a polyanionic shell: Synthesis, characterization, and application in aqueous biphasic hydrogenation

Core-crosslinked micelles (CCMs) with a hydrophilic polyanionic shell made of poly(sodium styrene sulfonate) chains, P(SS−Na+), a triphenylphosphine oxide-functionalized polystyrene core (TPPO@PSt) and crosslinked at the inner end of the polystyrene chains by diethylene glycol dimethacrylate (DEGDMA) were synthesized by reversible addition-fragmentation chain-transfer (RAFT) polymerization as a stable TPPO@CCM-A latex. One-pot synthesis of rhodium nanoparticles (RhNPs) by the reduction of [Rh(COD)(μ-Cl)]2 in the aqueous TPPO@CCM-A latex yielded a stable RhNP-TPPO@CCM-A latex without the need of additional stabilizer or base. This Rh-loaded latex was applied to the catalytic biphasic hydrogenation of styrene under mild conditions with complete selectivity towards ethylbenzene and corrected turnover frequencies (cTOFs) ranging from 3250 to 10,010 h−1 based on the surface atoms of the RhNPs. Importantly, the catalytic phase proved recyclable after product extraction, owing to the efficient retention of the RhNPs by the core TPPO ligands.

Validation of ZIP4 as a tumour-associated antigen for nanotargeting

Pancreatic ductal adenocarcinoma remains a highly aggressive and untreatable cancer. There is a need to develop a new PDAC-associated antigen-targeting drug delivery system to tackle this disease. We validated choosing ZIP4 as a putative target in PDAC theranostics. We developed a nanosystem composed of a fluorescent polystyrene core coated with gold nanoparticles onto which a ZIP4-specific polyclonal antibody is attached. The polystyrene core’s fluorescence properties allow the nanosystem tracking by intravital imaging. We also developed two ZIP4-expressing cell lines by stably transfecting HEK293 and RWP1 cells with a ZIP4-coding plasmid that simultaneously provides cells with puromycin resistance. We studied the cell internalisation of the as-synthesised nanoparticles and demonstrated that ZIP4-expressing HEK293 and ZIP4-expressing RWP1 cells tended to take up more ZIP4-targeting nanoparticles. Moreover, we observed that ZIP4-targeting nanoparticles accumulated more in ZIP4-expressing HEK293 and RWP1 tumours when injected intravenously in a subcutaneous xenograft and an orthotopic in vivo model, respectively. Furthermore, the administration of these nanoparticles did not induce any significant systemic toxicity as determined by histological analysis of all organs. Altogether, these results provide the first evidence of the feasibility of using a ZIP4-targeting nanosystem further to design efficient therapeutic and diagnostic tools for PDAC.

The Buffer Capacity of Polyelectrolyte Microcapsules Depends on the Type of Template.

One of the key physicochemical parameters of polyelectrolyte microcapsules (PMCs) is their buffer capacity (BC). The BC of the microcapsules allows for an assessment of the change in protonation state across the entire polyelectrolyte system, which directly impacts the buffer barrier of PMCs, as well as the stability and physical properties of their shell. However, the buffer capacity of PMCs and their behavior under changes in ionic strength and temperature can differ depending on the type of core used to form the microcapsules. As part of this study, we revealed the buffer capacity (BC) of polyelectrolyte microcapsules formed on polystyrene cores (PMCPs) and studied the influence of ionic strength and environmental temperature on the BC of these capsules. We found that the buffer capacity of PMCPs differs from the BC of water at a pH above 8; the addition of sodium chloride leads to an increase in buffer capacity in alkaline conditions, and conversely, thermal treatment leads to its decrease at a pH of 9. The results obtained are different from the BC of polyelectrolyte microcapsules formed on CaCO3 cores, which suggests a difference in the physicochemical properties of these types of capsules. The buffer capacity of polyelectrolyte microcapsules depends on the type of template used.

Structural Colors Derived from the Combination of Core–Shell Particles with Cellulose

Combining cellulose‐based components with functional materials is highly interesting in various research fields due to the improved strength and stiffness of the materials combined with their low weight. Herein, the mechanical properties of opal films are improved by incorporating cellulose fibers and microcrystalline cellulose. This is evidenced by the increase in tensile strength of 162.8% after adding 10 wt% of microcrystalline cellulose. For this purpose, core–shell particles with a rigid, crosslinked polystyrene core and a soft shell of poly(ethyl acrylate) and poly(ethyl acrylate‐co‐hydroxyethyl methacrylate) are synthesized via starved‐feed emulsion polymerization. The synthesized particles’ well‐defined shape, morphology, and thermal properties are analyzed using transmission electron microscopy, scanning electron microscopy, and differential scanning calorimetry measurements. Free‐standing mechanochromic opal films with incorporated cellulose and structural colors are obtained after processing the core–shell particles with cellulose via extrusion and the melt‐shear organization technique. The homogeneous distribution of the cellulose within the composite material is investigated using fluorescent‐labeled cellulose. The opal film's angle‐dependent structural color is demonstrated using reflection spectroscopy.

Robust and Durable Photonic Crystal with Liquid-Repellent Property for Self-Cleaning Coatings and Structural Colored Textiles.

Photonic crystal coatings with unique structural colors and self-cleaning properties have been providing an efficient way for substrate coloration. However, the enhancement of the robustness and durability of structural colored coatings to meet the requirements in diverse environments remains a challenging task. Here, to realize the application of photonic crystal films under various kinds of conditions, we present a poly(fluoroalkyl acrylate)-based colloidal photonic crystal (fCPC) coating. Fluorinated core-interlayer-shell (FCIS) colloidal particles of polystyrene (PS) core, poly(methyl methacrylate) (PMMA) interlayer, and poly(fluoroalkyl acrylate-ethyl acrylate-butyl acrylate) (P(FA-EA-BA)) shell copolymers have been first prepared by a stepwise emulsion polymerization. fCPCs with self-supporting property, reprocessing ability, friction resistance, as well as excellent wettability and liquid-repellent properties are successfully obtained via the bending-induced ordering technique (BIOT). When applied in antifouling applications, the fCPC film exhibits resistance against various oil and inorganic liquids. Furthermore, the fCPC coatings demonstrate their durability under outdoor conditions by maintaining stable color appearances during rainy and sunny conditions. Additionally, an electronic product adhered with the fCPC coatings is presented, which exhibits a surface that remains clean even after prolonged usage in comparison to the conventional CPC coating. Structural colored textiles with enhanced stability and functionalized liquid-repellent properties are achieved through a one-step process using FCIS particles. Therefore, the developed self-cleaning and comprehensive fCPC coatings capable of withstanding diverse conditions may open up new avenues for the advancement of structural coloration in decoration, vehicle, textile, and building.

Advancing triboelectric human machine interfaces with core-sheath nanocomposite fibres: Enhanced flexibility and motion identification via machine learning

The rapid development of triboelectric nanogenerators (TENGs) has led to sustainable sensing applications as triboelectric interfaces for activity/pattern recognition in human machine interaction (HMI). In this work, core-sheath nanofibres were synthesized and employed as triboelectric materials for constructing new TENGs. These electrospun fibres of novel design consist of a nanocomposite core comprised of polystyrene (PS) and molybdenum disulfide (MoS2) nanoplatelets, and a sheath made of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Compared to high performance TENGs based on neat PVDF-HFP nanofibres tribolayer, these new TENGs achieved open circuit voltage of 1944 V and short-circuit current of 40.3 μA, yielding a total improvement of 284% and 783%, respectively, attributed from the highly efficient charge storage and binding capabilities from the MoS2 nanoplatelets and the PS core. To harness the remarkable performances of these new TENGs, a touch input component was developed, designed to work in conjunction with machine learning algorithms. The triboelectric interfaces exhibited high accuracy in user identification, capable of recognizing individual users with up to 86% average accuracy, under identical press patterns applied by different users. This paves the way for future development of machine learning assisted HMI enabled by TENGs for next generation sustainable communication networks.

Synthesis of Raspberry-like Nanoparticles via Surface Grafting of Positively Charged Polyelectrolyte Brushes: Colloidal Stability and Surface Properties.

A method to synthesize stable, raspberry-like nanoparticles (NPs), using surface grafting of poly(glycidyl methacrylate) (PGMA) brushes on a polystyrene (PS) core with varying grafting densities, is reported. A two-step functionalization reaction of PGMA epoxide groups comprising an amination step first using ethylene diamine and then followed by a quaternization using glycidyltrimethylammonium chloride generates permanently and positively charged polyelectrolyte brushes, which result in both steric and electrostatic stabilization. The dispersion stability of the brush-bearing NPs is dramatically improved compared to that of the pristine PS core in salt solutions at ambient (25 °C) and elevated temperatures (60 °C). Additionally, the grafted polyelectrolyte chains undergo a reversible swelling in the presence of different ionic strength (IS) salts, which modulate the surface properties, including roughness, stiffness, and adhesion. An atomic force microscope under both dry and wet conditions was used to image conformational changes of the polyelectrolyte chains during the swelling and deswelling transitions as well as to probe the nanomechanical properties by analyzing the corresponding force-sample separation curves. The quaternized polyelectrolyte brushes undergo a conformational transition from a collapsed state to a swelled state in the osmotic brush (OB) regime triggered by the osmotic gradient of mobile ions to the interior of the polymer chain. At IS ∼ 1 M, the brushes contract and the globules reform (salted brush state) as evidenced by an increase in the surface roughness and a reduction in the adhesion of the brushes. Beyond IS ∼ 1 M, quartz crystal microbalance with dissipation monitoring measurements show that salt uptake continues to take place predominantly on the exterior surface of the brush since salt adsorption is not accompanied by a size increase as measured by dynamic light scattering. The study adds new insights into our understanding of the behavior of NPs bearing salt-responsive polyelectrolyte brushes with adaptive swelling thresholds that can ultimately modulate surface properties.

Poly(4-vinylpyridine) and Poly(methacrylic acid) Particle Architectures for pH-Responsive and Mechanochromic Opal Films.

While stimuli-responsive structural colors are commonly found in nature, mimicking these in artificial materials is challenging. Dynamically switchable and tunable coloration, however, is in high demand in widespread fields of applications, including advanced display and monitoring technologies, smart sensing, and anticounterfeiting. This work reports a scalable protocol for the synthesis of tailor-made core-shell particles and subsequent processing to opal films with iridescent, pH-responsive, and mechanochromic structural color. Novel monodisperse core-shell architectures based on hard polystyrene core particles are synthesized via stepwise emulsion polymerization in a starved-feed mode. The incorporation of 4-vinylpyridine and methacrylic acid as functional comonomers in the soft particle shell facilitates pH-responsive swelling and deswelling. Mechanically stable and well-ordered colloidal crystal films are obtained by the self-assembly of the particles during processing with the powerful melt-shear organization technique. Thereby obtained opal films show Bragg-scattering at the colloidal crystalline structure and exhibit brilliant green-turquoise to blue-violet reflection colors, dependent on the angle of view and illumination. Upon changes in the pH value or mechanical deformation, the reflected wavelength shifts by more than 100 nm, leading to intriguing changes in the visible structural color. Excellent reversibility is achieved by the subsequent application of a convenient UV cross-linking strategy, corroborating the high application potential of these advanced functional materials.

Facile fabrication of carbon nanotube hollow microspheres as a fiber coating for ultrasensitive solid-phase microextraction of phthalic acid esters in tea beverages.

The efficient extraction of phthalic acid esters (PAEs) is challenging due to their extremely low concentration, complicated matrices and hydrophilicity. Herein, hollow microspheres, as an ideal coating, possess significant potential for solid-phase microextraction (SPME) due to their fascinating properties. In this study, multiwalled carbon nanotube hollow microspheres (MWCNT-HMs) were utilized as a fiber coating for the SPME of PAEs from tea beverages. MWCNT-HMs were obtained by dissolving the polystyrene (PS) cores with organic solvents. Interestingly, MWCNT-HMs well maintain the morphology of the MWCNTs@PS precursors. The layer-by-layer (LBL) assembly of MWCNTs on PS microsphere templates was achieved through electrostatic interactions. Six PAEs, di-ethyl phthalate (DEP), di-iso-butyl phthalate (DIBP), di-n-butyl phthalate (DBP), benzyl butyl phthalate (BBP), di-2-ethylhexyl phthalate (DEHP) and di-n-octyl phthalate (DOP), were selected as target analytes for assessing the efficiency of the coating for SPME. The stirring rate, sample solution pH and extraction time were optimized by using the Box-Behnken design. Under optimal working conditions, the proposed MWCNT-HMs/SPME was coupled with gas chromatography-tandem mass spectrometry (GC-MS/MS) to achieve high enrichment factors (118-2137), wide linearity (0.0004-10 μg L-1), low limits of detection (0.00011-0.0026 μg L-1) and acceptable recovery (80.2-108.5%) for the detection of PAEs. Therefore, the MWCNT-HM coated fibers are promising alternatives in the SPME method for the sensitive detection of PAEs at trace levels in tea beverages.

Investigation of mechanical behavior of glass fiber reinforced extruded polystyrene core material composites.

Layered composites are composite materials created by combining different layers of materials. Each layer can possess unique properties, often tailored to meet specific application or design requirements. These composites have found applications in various sectors due to their features, which include lightness, excellent impact properties, and customization according to specific application areas. In this study, glass fiber reinforced polymer foam core layered composite materials were produced. EPS polymer foam was used as the core material. During production, polymer foams and fibers were bonded to the upper and lower sides of the foams using resin. Samples were produced with 4 and 6 layers on both sides, totaling 8 and 12 layers, respectively. The vacuum bagging method was employed in production, utilizing the manual laying technique. Upon completion of production, the materials were cut into sizes conforming to standards and converted into samples. Subsequently, three-point bending and low-speed impact tests were conducted on the produced samples. As a result of the impact tests, perforation occurred in the 8-layer samples of 200 g m-2 glass fiber composites, while rebound was observed in the 12-layer samples. Although more deformation occurred in the 8-layer glass fiber composites of 300 g m-2 than in the 12-layer samples, both sets of experiments resulted in rebound. Similar results to the impact tests were obtained in three-point bending tests, with higher strengths observed in the 12-layer samples compared to the 8-layer samples. Composite samples with fiber layers of 300 g m-2 exhibited better performance than samples with 200 g m-2 fibers.

Investigation of the Damping Abilities of Sheep Wool Reinforced Expanded Polystyrene Core Layer Composites at Different Energies

Investigation of the Damping Abilities of Sheep Wool Reinforced Expanded Polystyrene Core Layer Composites at Different Energies

Construction of Steady Amorphous Colloidal Array Patterns via Infiltration-Driven Assembly of Core-Shell Microparticles followed by Short-Time Heating.

Although core-shell microparticles with a hard core and soft shell are often used to fabricate photonic crystal films, they are rarely applied to construct steady amorphous colloidal array (ACA) patterns. In this work, a series of monodisperse core-shell microparticles with a polystyrene (PS) core and poly(methyl methacrylate-butyl acrylate) (P(MMA-BA)) shell have been successfully synthesized, and the glass transition temperatures (Tg) of the shell layer have been well regulated. The synthesized core-shell microparticles were then used to fabricate ACA patterns via a convenient infiltration-driven assembly method. The results showed that the Tg of the shell significantly affected the microstructure of the amorphous colloidal arrays (ACAs). During the assembly process, the microparticles quickly contacted each other and the lower-Tg shells could merge with each other to form a continuous film. In this situation, the PS core was embedded and ranked in the P(MMA-BA) film, and both the refractive index contrast and order degree of the colloidal array became relatively low, resulting in a poor structural color. However, when the Tg of the shell layer was moderately high, a short-range ordered array was prepared via infiltration-driven assembly, thereby displaying a bright structural color. More importantly, the shell layers could merge with each other to some extent after short-time heating, resulting in fine mechanical stability. In brief, this study provides a facile and environmental approach to construct steady ACA patterns, which is promising in printing and painting industries.

Dual Stimuli‐Responsive Ternary Core‐Shell Polystyrene@Pnipam‐Pedot Latexes

AbstractThe ability of stimuli‐responsive materials to respond to external stimuli depends on their intra‐ and intermolecular interactions, which, in turn, are governed by changes in the material composition. Here, the importance of these factors for new heat and light‐sensitive latexes of core‐shell nanoparticles is reported with the polystyrene core, the poly(N‐isopropylacrylamide) (PNIPAM) shell containing doped poly(3,4‐ethylenedioxythiophene) (PEDOT). It is found that hydrogen bonding, C═O─π aromatic, hydrophilic‐hydrophobic interactions in the shell cause conformational changes in PNIPAM similar to those occurring in the PNIPAM coil‐globule transition. Depending on the EDOT:PS@PNIPAM feed ratio and the PEDOT content in PNIPAM shells, these interactions and changes affect nanoparticle sizes and are responsible for shifting the lower critical solution temperature (LCST) of PNIPAM in the shell from 32.1 to 33.9 °C. The core‐shell morphology of nanoparticles is maintained only for latexes with EDOT feed to ≈9 wt.%. At the higher EDOT content, PNIPAM shells are destroyed. Synthesized PS@PNIPAM‐PEDOT latexes demonstrate temperature‐dependent behavior and produce a photothermal effect under NIR irradiation, which allows for a rise of their temperature above LCST. This dual stimuli (heat and light) responsiveness suggests an important possibility for these latexes to be used for drug or diagnostic agent delivery.

Confinement of Rh nanoparticles in triphenylphosphine oxide-functionalized core-crosslinked micelles for aqueous biphasic hydrogenation catalysis

The introduction of phosphine oxide as anchoring groups in the hydrophobic core of amphiphilic star-block copolymers leads to greatly improved confinement of rhodium nanoparticles (RhNPs) inside the nanoreactors with a benefit in aqueous biphasic catalysis. The copolymers are specially designed core-crosslinked micelles (CCMs) forming a stable latex by reversible addition-fragmentation chain-transfer (RAFT) polymerization. They possess a hydrophilic shell made of polycationic 4-vinyl-N-methylpyridinium iodide P(4VPMe+I−) chains, a triphenylphosphine oxide (TPPO)-functionalized polystyrene core and are crosslinked at the inner end of the polystyrene chains by diethylene glycol dimethacrylate (DEGDMA) (TPPO@CCM-C). Ex-situ synthesized RhNPs readily cross the hydrophilic shell and remain anchored within the CCM nanoreactor cores. The RhNP-loaded TPPO@CCM-C latex was applied as catalyst in the hydrogenation of styrene under mild conditions with complete selectivity towards ethylbenzene and average turnover frequency (TOF) up to 12000 h−1, corresponding to a corrected TOF (cTOF) up to 16800 h−1 based on only surface atoms of the RhNPs. Moreover, the catalytic phase proved recyclable after product extraction with diethyl ether, demonstrating efficient retention of the RhNPs by the core TPPO ligands. Although the activity decreased after the first catalytic run, it converged to a stable average TOF of ca. ∼1025 h−1 (cTOF of ca. ∼1440 h−1), which was similar to that of an extensively pre-washed RhNP-TPPO@CCM-C latex. This phenomenon is attributed to a promoter effect of adsorbed ligands, which were used as stabilizer for the RhNPs synthesis and were gradually removed during the work-up washings between recycles.

Synthesis of amine functionalized SiO2 microspheres loaded polymeric hydrogel and its application for simultaneous eviction of divalent metal ions (Pb2+, Cd2+, Cu2+ and Ni2+)

Recovery of divalent cationic elements from aquatic system is deliberated as reconciliation of rising industrial growth and access to quality drinking water. Herein we report tactically designed amino functionalized silica core-shell nanoparticle loaded polymeric hydrogel network as benchmark sorbent for divalent metal ions (Pb2+, Cd2+, Cu2+, Ni2+). The simple fabrication method for silica core-shell microspheres involves sol-gel synthesis of the polystyrene (PS) core, afterwards the formation of the silica shell by hydrolysis and condensation reaction, and finally the dissolution of the PS core. The surface of synthesized SiO2 microspheres was amine functionalized before being impregnated within a alginate matrix of polymer to generate amino functionalized SiO2 microsphere loaded polymeric hydrogel [NH2–SiO2MS-Ca-Alg] beads. Combining functionalized silica into polymeric hydrogel structure resulted extraordinary sorption capacities for divalent metal ions [191.4, 70.7, 64.9 and 35.8 mg g−1 respectively for Pb, Cd, Cu and Ni]. Density functional theory calculations were carried out to find out binding energies, preferred binding site of all four studied ions and structural changes due to their sorption. Structural evidence derived from experimental observations corroborate with the DFT analysis and speciation diagram of the divalent metal ion species. Plausible mechanistic pathway and differential uptake of four divalent metal ions were explained based on both experimental findings and theoretical studies. Developed NH2–SiO2 MS-Ca-Alg beads offered outstanding selectivity towards four divalent cations in a single prescription, excellent employability under ambient conditions without affecting essential water quality parameters which are significant breakthroughs for sustainable water remediation applications.

Dial-In Synthesis of 'Polymer Opal' Core-Interlayer-Shell Composite Nanoparticles.

The emulsion polymerization process via which core-interlayer-shell polymer nanoparticles are synthesized is engineered to offer a crucial control of the eventual size and monodispersity of the polystyrene (PS) cores. We examine the role of key experimental parameters, optimizing the temperature, reactant purity, and agitation (stirring) rate. The subsequent addition of a poly(methyl-methacrylate) (PMMA) grafting layer and a poly(ethyl-acrylate) (PEA) shell layer produces composite particles, which are shear-orderable into opaline films, known as 'polymer opals'. We thus demonstrate pathways toward a 'dial-in' process, where the time taken to obtain the target core size is mapped to the expected resultant structural color. At reaction temperatures of 60 and 70 °C, viable conditions are found where all syntheses give an excellent level of monodispersity (polydispersity index < 0.02), suitable for interlayer and shell growth. These reports may be readily applied to a wider industrial scale fabrication pipeline for these polymeric photonic materials.

New hard-template strategy for the synthesis of [formula omitted]-Fe[formula omitted]O[formula omitted] hollow-spheres

A new route to manufacture hematite (α-Fe2O3) hollow spheres with a diameter of approximately 165 ± 29 nm is presented. The proposal is based on the use of polystyrene spheres as a hard template and ethylene glycol as a solvent. In the intermediate stage of the synthesis, the PS@Fe(OH)3 sample was manufactured. For this sample, transmission electron microscopy and scanning electron microscopy confirmed the good uniformity of the polystyrene core coating, which has a thickness of approximately 12 ± 5 nm. EDS mapping confirmed the presence of iron and oxygen. The shell composition (α-FeOOH) was confirmed by Raman spectroscopy and FTIR. In the final stage of the synthesis, the Void@Fe2O3 sample was obtained. For this sample, core removal and the shell thickness (16 ± 5 nm) were confirmed by electron microscopy. EDS mapping confirmed the presence of iron and oxygen, in addition to indicating the complete removal of the polystyrene core. XRD and Raman measurements confirmed that the shell is constituted of hematite with traces of iron hydroxide. These results demonstrate the success of the adopted strategy for the synthesis of hematite hollow spheres.

Mechanical Efficiency and Quality Control Preliminary Analysis of Incompletely Bonded Wood-Based Sandwich Panels

Wood-based sandwich panels are building products composed of two skins attached to a lightweight continuous core in which at least one skin is made of wood-based products, contributing to the use of renewable forest goods. Since the connection between the skins and the core is often provided by adhesive bonding, its characteristics affect the mechanical behavior of the sandwich and, therefore, must be thoroughly assessed. Full adhesion is often considered the standard situation, although some batches of the commercial product show incompletely glued surfaces, and scarce data is available with regard to their bonding performance. For this reason, analyses were performed using tensile tests with a load perpendicular to the skins and specific shear tests with a load parallel to the longitudinal direction of the panel. The test samples were obtained from wood-based sandwich panels with extruded polystyrene cores and different skin materials. The tensile tests proved to be suitable only for panels with adequate skin material cohesion, their functionality improving as a control method when the glued surface percentage assessment is used together with the tensile strength. The results of the shear tests provided non-linear models relating the effect of the glued surface to the mechanical properties, revealing that the mechanical efficiency of the incompletely bonded specimens is better than that which might be expected if the core only worked in proportion to the glued surface, due to the help of the adjoining non-glued core material.

Imaging Radial Distribution Functions of Complex Particles by Relayed Dynamic Nuclear Polarization.

The physical properties of many modern multi-component materials are determined by their internal microstructure. Tools capable of characterizing complex nanoscale architectures in composite materials are, therefore, essential to design materials with targeted properties. Depending on the morphology and the composition, structures may be measured by laser diffraction, scattering methods, or by electron microscopy. However, it can be difficult to obtain contrast in materials where all the components are organic, which is typically the case for formulated pharmaceuticals, or multi-domain polymers. In nuclear magnetic resonance (NMR) spectroscopy, chemical shifts allow a clear distinction between organic components and can in principle provide the required chemical contrast. Here, we introduce a method to obtain radial images of the internal structure of multi-component particles from NMR measurements of the relay of nuclear hyperpolarization obtained from dynamic nuclear polarization. The method is demonstrated on two samples of hybrid core-shell particles composed of a core of polystyrene with a shell of mesostructured silica filled with the templating agent CTAB and is shown to yield accurate images of the core-shell structures with a nanometer resolution.

A Floating Integrated Solar Micro‐Evaporator for Self‐Cleaning Desalination and Organic Degradation

AbstractSafe and clean freshwater harvesting from (organic‐containing) saline or wastewater holds great potential for mitigating water scarcity and pollution, but remains challenging. Herein, a floating photothermal/catalytic‐integrated interfacial micro‐evaporator (g‐C3N4@PANI/PS) is reported as a proof‐of‐concept multifunctional scavenger evaporator system (MSES) to achieve both solar‐driven complete desalination and organic degradation. The spherical porous lightweight polystyrene core, incorporated with a black surface functional layer (g‐C3N4@PANI), enables the hybrid micro‐evaporator to naturally float and thereby collectively self‐assemble under surface tension for interfacial evaporation, which achieves preeminent self‐cleaning for complete salt/solute separation and efficient organic photodegradation under rotation. Remarkably, the floating micro‐evaporator achieves a high solar‐vapor conversion efficiency of ≈90% with high interfacial energy localization and provides abundant active photocatalytic sites on the interface, which is further enhanced by interfacial photothermal cooperation. High photo‐driven degradation efficiencies of 99% for nonvolatile organic compounds (non‐VOC) bisphenol A and 95% for VOC phenol in wastewater are achieved. An outdoor comprehensive solar water treatment test toward organic‐containing high‐salinity sewage verifies the feasibility of MSES for sustainable freshwater harvesting (1.3 kg m−2 h−1), downstream salt recovery, and organic degradation. This strategy may inspire an integrated solution of water scarcity, clean energy, and environmental pollution toward carbon neutrality.